1-Bromo-3-(1-propen-2-yl)benzene

≥95%

Reagent Code: #154436
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CAS Number 25108-58-1

science Other reagents with same CAS 25108-58-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.07 g/mol
Formula C₉H₉Br
badge Registry Numbers
MDL Number MFCD20384534
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromine group allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic compounds. The isopropenyl moiety provides a site for further functionalization, making it valuable in the development of fine chemicals and specialty materials. Commonly employed in research settings to build molecular diversity in medicinal chemistry projects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,330.00
inventory 1g
10-20 days ฿7,600.00
inventory 5g
10-20 days ฿22,330.00

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1-Bromo-3-(1-propen-2-yl)benzene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromine group allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic compounds. The isopropenyl moiety provides a site for further functionalization, making it valuable in the development of fine chemicals and specialty materials. Commonly employed in research settings to build molecular diversity in medicinal chemis

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromine group allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic compounds. The isopropenyl moiety provides a site for further functionalization, making it valuable in the development of fine chemicals and specialty materials. Commonly employed in research settings to build molecular diversity in medicinal chemistry projects.

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